German Institute of Human Nutrition Potsdam-Rehbrucke, Nuthetal, Germany.
Obes Facts. 2008;1(6):292-7. doi: 10.1159/000176064. Epub 2008 Dec 2.
We have previously reported that a high-fat, carbohydrate-free diet prevents diabetes and beta-cell destruction in the New Zealand Obese (NZO) mouse strain. Here we investigated the effect of diets with and without carbohydrates on obesity and development of beta-cell failure in a second mouse model of type 2 diabetes, the db/db mouse.
When kept on a carbohydrate-containing standard (SD; with (w/w) 5.1, 58.3, and 17.6% fat, carbohydrates and protein, respectively) or high-fat diet (HFD; 14.6, 46.7 and 17.1%), db/db mice developed severe diabetes (blood glucose >20 mmol/l, weight loss, polydipsia and polyurea) associated with a selective loss of pancreatic beta-cells, reduced GLUT2 expression in the remaining beta-cells, and reduced plasma insulin levels. In contrast, db/db mice kept on a high-fat, carbohydrate-free diet (CFD; with 30.2 and 26.4% (w/w) fat or protein) did not develop diabetes and exhibited near-normal, hyperplastic islets in spite of a morbid obesity (fat content >60%) associated with hyperinsulinaemia.
These data indicate that in genetically different mouse models of obesity-associated diabetes, obesity and dietary fat are not sufficient, and dietary carbohydrates are required, for beta-cell destruction.
我们先前报道了高脂肪、无碳水化合物饮食可预防新西兰肥胖(NZO)小鼠糖尿病和胰岛β细胞破坏。在此,我们研究了含碳水化合物和不含碳水化合物的饮食对另一种 2 型糖尿病小鼠模型 db/db 小鼠肥胖和胰岛β细胞衰竭发展的影响。
当 db/db 小鼠分别摄入含碳水化合物的标准饮食(SD;分别含有(w/w)5.1%、58.3%和 17.6%的脂肪、碳水化合物和蛋白质)或高脂肪饮食(HFD;14.6%、46.7%和 17.1%的脂肪、碳水化合物和蛋白质)时,会发生严重的糖尿病(血糖>20mmol/L、体重减轻、多饮和多尿),伴有胰岛β细胞选择性丧失、剩余胰岛β细胞 GLUT2 表达减少和血浆胰岛素水平降低。相比之下,db/db 小鼠摄入高脂肪、无碳水化合物饮食(CFD;分别含有 30.2%和 26.4%(w/w)的脂肪或蛋白质)不会发生糖尿病,尽管存在与高胰岛素血症相关的病态肥胖(脂肪含量>60%),但其胰岛仍呈增生状态,近乎正常。
这些数据表明,在肥胖相关糖尿病的遗传不同的小鼠模型中,肥胖和饮食中的脂肪不足以导致胰岛β细胞破坏,还需要饮食中的碳水化合物。